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DDX10P1 DEAD-box helicase 10 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 100421371, updated on 25-Jan-2022

Summary

Official Symbol
DDX10P1provided by HGNC
Official Full Name
DEAD-box helicase 10 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:44960
See related
Ensembl:ENSG00000237135 AllianceGenome:HGNC:44960
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See DDX10P1 in Genome Data Viewer
Location:
10p11.23
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 10 NC_000010.11 (30919008..30921130, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (31207937..31210059, complement)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene supervillin family member 2, pseudogene Neighboring gene long intergenic non-protein coding RNA 2644 Neighboring gene zinc finger protein 438 Neighboring gene uncharacterized LOC105376481 Neighboring gene uncharacterized LOC105376482 Neighboring gene uncharacterized LOC105376483

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_025423.1 

    Range
    101..2223
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000010.11 Reference GRCh38.p13 Primary Assembly

    Range
    30919008..30921130 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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